• Carry out the pharmaceutical development of new formulations and Bimeda's formulas; prepare development and stability test reports, do bibliographic research.

• Develop, review and update product documentation for the transfer of production technology.

• Control the entry and exit of the climatic chambers and send the samples to Quality Control.

• Monitor the stability studies carried out by the company or third parties and carry out critical analysis of the results.

• Make protocols and reports of stability tests of products and stability reports of monitoring of registered products.

• Carry out the preparation of Standard Operating Procedures and keep them in force in the area of Development.

• Monitor the progress of clinical trials.

General Service